
Clinical Trial Specialist
2 weeks ago
We are seeking a skilled Clinical Research Associate to join our team. This is an exciting opportunity for individuals who are passionate about scientific rigor and clinical development.
The successful candidate will be responsible for monitoring global clinical trials, ensuring the integrity of data submitted on Case Report Forms, and managing resources efficiently.
Key Responsibilities:
- Conduct site visits, monitor trial progress, and ensure compliance with regulatory requirements
- Verify informed consent procedures and protocol requirements
- Manage study files, conduct pre-study and initiation visits, and liaise with vendors
- Prepare accurate and timely trip reports, track Serious Adverse Event (SAE) reporting, and process production of reports
Requirements:
- University or college degree, or certification in a related allied health profession from an appropriately accredited institution
- Demonstrated experience of at least 18 months in onsite monitoring global clinical trials from SIV to Close-out
- Understanding of local regulatory guidelines
- Ability to travel interstate and work in a hybrid environment
About this Role:
This is a dynamic opportunity for someone looking to advance their career in clinical research. Our team is dedicated to delivering high-quality solutions to our customers, and we are committed to supporting our staff in their professional growth.
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